期刊论文详细信息
BMC Research Notes
A method for improved clustering and classification of microscopy images using quantitative co-localization coefficients
Jeremy C Simpson2  Kathleen M Curran1  Kenan Handzic2  Vasanth R Singan1 
[1] School of Medicine and Medical Science, University College Dublin, Dublin 4, Belfield, Ireland;School of Biology and Environmental Science & Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin 4, Belfield, Ireland
关键词: Rab proteins;    Clustering;    Texture features;    Image analysis;    Quantitative co-localization;   
Others  :  1166338
DOI  :  10.1186/1756-0500-5-281
 received in 2012-03-06, accepted in 2012-06-08,  发布年份 2012
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【 摘 要 】

Background

The localization of proteins to specific subcellular structures in eukaryotic cells provides important information with respect to their function. Fluorescence microscopy approaches to determine localization distribution have proved to be an essential tool in the characterization of unknown proteins, and are now particularly pertinent as a result of the wide availability of fluorescently-tagged constructs and antibodies. However, there are currently very few image analysis options able to effectively discriminate proteins with apparently similar distributions in cells, despite this information being important for protein characterization.

Findings

We have developed a novel method for combining two existing image analysis approaches, which results in highly efficient and accurate discrimination of proteins with seemingly similar distributions. We have combined image texture-based analysis with quantitative co-localization coefficients, a method that has traditionally only been used to study the spatial overlap between two populations of molecules. Here we describe and present a novel application for quantitative co-localization, as applied to the study of Rab family small GTP binding proteins localizing to the endomembrane system of cultured cells.

Conclusions

We show how quantitative co-localization can be used alongside texture feature analysis, resulting in improved clustering of microscopy images. The use of co-localization as an additional clustering parameter is non-biased and highly applicable to high-throughput image data sets.

【 授权许可】

   
2012 Singan et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Simpson JC, Pepperkok R: The subcellular localization of the mammalian proteome comes a fraction closer. Genome Biol 2006, 7:222. BioMed Central Full Text
  • [2]Hamilton NA, Teasdale RD: Visualizing and clustering high throughput sub-cellular localization imaging. BMC Bioinformatics 2008, 9:81. BioMed Central Full Text
  • [3]Glory E, Murphy RF: Automated subcellular location determination and high-throughput microscopy. Dev Cell 2007, 12:7-16.
  • [4]Horvath P, Wild T, Kutay U, Csucs G: Machine learning improves the precision and robustness of high-content screens: using nonlinear multiparametric methods to analyze screening results. J Biomol Screen 2011, 16:1059-1067.
  • [5]Haralick RM: Statistical and structural approaches to texture. Proc IEEE 1979, 67:786-804.
  • [6]Carpenter AE: Extracting rich information from images. Methods Mol Biol 2009, 486:193-211.
  • [7]Simpson JC: Screening the secretion machinery: High throughput imaging approaches to elucidate the secretory pathway. Sem Cell Dev Biol 2009, 20:903-909.
  • [8]Singan VR, Jones TR, Curran KM, Simpson JC: Dual channel rank-based intensity weighting for quantitative co-localization of microscopy images. BMC Bioinformatics 2011, 12:407. BioMed Central Full Text
  • [9]Stenmark H: Rab GTPases as coordinators of vesicle traffic. Nat Rev Mol Cell Biol 2009, 10:513-525.
  • [10]Campany A, Leiva N, Damiani MT: Golgi-associated Rab14, a new regulator for Chlamydia trachomatis infection outcome. Commun Integr Biol 2011, 4:590-593.
  • [11]Zheng JY, Koda T, Fujiwara T, Kishi M, Ikehara Y, Kakinuma M: A novel Rab GTPase, Rab33B, is ubiquitously expressed and localized to the medial Golgi cisternae. J Cell Sci 1998, 111:1061-1069.
  • [12]Schluter OM, Khvotchev M, Jahn R, Sudhof TC: Localization versus function of Rab3 proteins. Evidence for a common regulatory role in controlling fusion. J Biol Chem 2002, 277:40919-40929.
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